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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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MIR065 — 2 UDI-DI variants, MDR

MD Atlas
MIR - Medical International Research S.p.A.

Data from EUDAMED, last updated May 30, 2026

MIR065

805299032065O4Z

2 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIa

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: MIR - Medical International Research S.p.A.

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 805299032065O4Z
Device name: —
Device model: MIR065
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: May 21, 2026

Manufacturer & authorised representative

Manufacturer

Name: MIR - Medical International Research S.p.A.
SRN: IT-MF-000014026
Country: Italy
Email: mir@spirometry.com
Phone: +39 06 22754777

Variants by status

UDI-DI variants

2 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KS2RTWK57HVAT45AJXGD11RX

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

911120 - 911120B008052990321704
911125 - 911125B0 - 911125P1 - 911125P0 - 911125S1 - 911125S008052990321711